Lifestyle Intervention and Testosterone Replacement in Obese Seniors (LITROS)
Primary Purpose
Obesity and Hypogonadism
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Testosterone
Lifestyle Therapy
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Obesity and Hypogonadism focused on measuring Obesity, Hypogonadism, Frailty
Eligibility Criteria
Inclusion Criteria:
Subjects will be
- older (65-85 yr)
- obese (BMI 30 kg/m2 or greater) Veteran men with low testosterone (less than 300 mg/dL) as defined by the Endocrine Society
- mild to moderately frail
- must have stable weight (~not less than or more than 2 kg) during the last 6 months
- sedentary (regular exercise less than 1 h/week or less than 2x/week for the last 6 months)
Exclusion Criteria:
- Any major chronic diseases, or any condition that would interfere with exercise or dietary restriction, in which exercise or dietary restriction are contraindicated, or that would interfere with interpretation of results.
Examples include, but are not limited to:
- cardiopulmonary disease (e.g. recent myocardial infarction (MI), unstable angina, stroke etc) or unstable disease (e.g. CHF)
- severe orthopedic/musculoskeletal or neuromuscular impairments
- visual or hearing impairments
- cognitive impairment (Mini Mental State Exam Score less than 24)
- current use of bone active drugs
- uncontrolled diabetes (i.e. fasting blood glucose more than 140 mg/dl and/or HbA1c greater than 9.5%).
Any contraindications to testosterone supplementation
- history of prostate or breast cancer
- history of testicular disease
- untreated sleep apnea
- hematocrit more than 50%
- prostate-related findings of palpable nodule on exam, a serum PSA of 4.0 ng/ml or greater
- International Prostate Symptom Sore more than 19
- history of venous thromboembolism
- Osteoporosis or a BMD T-score of -2.5 in the lumbar spine or total hip as well as those patients with a history of osteoporosis-related fracture (spine, hip, or wrist)
Sites / Locations
- Michael E. DeBakey VA Medical Center, Houston, TX
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Testosterone plus Lifestyle Therapy
Placebo plus Lifestyle Therapy
Arm Description
Testosterone replacement in combination with behavioral diet to induce ~10% weight loss + supervised aerobic and exercise training
Placebo in combination with behavioral diet to induce ~10% weight loss and supervised aerobic and exercise training
Outcomes
Primary Outcome Measures
Change in the Physical Performance Test
The primary functional outcome is the modified physical performance test, which includes seven standardized tasks (walking 50 ft, putting on and removing a coat, picking up a penny, standing up from a chair, lifting a book, climbing one flight of stairs, and performing a progressive Romberg tests) plus two additional tasks (climbing up and down four flights of stairs and performing a 360-degree turn). The score for each task ranges form 0 to 4; a perfect score is 36. Higher scores indicate better physical function.
Secondary Outcome Measures
Change in Endurance Capacity
Assessed by measuring peak oxygen consumption using indirect calorimetry during a treadmill exercise stress test
Change in Functional Status
Assessed by the Functional Status Questionnaire. Score range: 0 to 36 with higher scores indicating better functional status
Provides information of the participants ability to perform activities of daily living.
Change in Body Weight
Measured after an overnight fast using calibrated scales
Change in Lean Body Mass
Assessed by using dual-energy x-ray absorptiometry
Change in Fat Mass
Assessed by using dual-energy x-ray absorptiometry
Change in Thigh Muscle Volume
Assessed by using magnetic resonance imaging
Thigh Fat Volume
Volume of fat in the thigh by measured by magnetic resonance imaging
Change in Total Hip Bone Mineral Density
Assessed by using dual-energy x-ray absorptiometry
Change in Lumbar Spine Bone Mineral Density
As measured by Dual energy x-ray absorptiometry
Change in Muscle Strength
assessed by total1-repetition maximum (the maximal weight lifted at one time; the totals are the sum of the maximal weights lifted in the biceps curl, bench press, 387 seated row, knee extension, knee flexion, and leg press exercises).
Change in Static Balance
assessed by one leg limb stance
Change in Dynamic Balance
Assessed by using the obstacle course
Change in Gait Speed
Determined by measuring the time needed to walk 25 ft.
Change in Composite Cognitive Z-score
Test of overall cognitive performance formed by averaging the standardized scores for several domains of cognitive function (attention, memory, executive, language, global). Higher scores indicate better cognitive status.
The Z-score indicates the number of standard deviations away from the mean. A Z-score of 0 is equal to the mean of the baseline scores (units on a scale). Negative numbers indicate values lower than the reference population and positive numbers indicate values higher than the reference population
Change in Modified Mini-mental Exam
Test of global cognition with components for orientation, registration, attention, language, praxis, and immediate and delayed memory. Score ranges from 0 to 100 with higher scores indicate better cognition.
Stroop Interference
Assess the ability to inhibit cognitive interference that occurs when the processing of a specific stimulus feature impedes the simultaneous processing of a second stimulus attribute, well-known as the Stroop Effect.
Minimum score is 0, there is no maximum value. Higher scores indicate better outcome.
Change in Word List Fluency
Measure of verbal production, semantic memory, and language. Minimum score is 0, there is no maximum value. Higher scores indicate better outcome.
Change in Ray Auditory Verbal Learning Test
The Rey Auditory Verbal Learning Test (RAVLT) evaluates a wide diversity of functions: short-term auditory-verbal memory, rate of learning, learning strategies, retroactive, and proactive interference, presence of confabulation of confusion in memory processes, retention of information.
Minimum score is 0, there is no maximum value. Higher scores indicate better outcome.
Change in Trail A
Test of visuospatial scanning, speed of processing, mental flexibility, and executive function (with a greater focus on attention).
Minimum score is 0, there is no maximum value. Higher scores indicate better outcome.
Change in Trail B
Test of visuospatial scanning, speed of processing, mental flexibility, and executive function (with a focus on executive function)
Minimum score is 0, there is no maximum value. Higher scores indicate better outcome.
Change in Symbol Digital Modalities Test
Assesses key neurocognitive functions that underlie many substitution tasks, including attention, visual scanning, and motor speed.
Minimum score is 0, there is no maximum value. Higher scores indicate better outcome.
Change in Trabecular Bone Score
The trabecular bone score is a measure of bone texture correlated with bone microarchitecture and a marker for the risk of osteoporosis.
Minimum score is 0, there is no maximum value. Higher scores indicate better bone microarchitecture.
Change in C-terminal Telopeptide
biochemical marker of bone turnover (bone resorption) as measured by immunoassay technique
Change in N-terminal Propeptide of Type I Procollagen
Biochemical marker of bone turnover (bone formation) as measured by radioimmunoassay technique
Change in Insulin Growth Factor-1
Measured by immunoassay methodology
Change in Trabecular Bone Score (Trabecular Bone Quality)
assessed by trabecular bone score (TBS), a newly developed index for assessing trabecular bone quality and fracture risk.
TBS is a bone texture parameter that quantifies cancellous bone microachitecture, which is key in determining bone strength and resistance to fracture, by computing raw data from dual energy x-ray absorptiometry of the lumbar spine.
There are no minimum or maximum values. Higher scores mean better outcome.
Change in Levels of 25-hydroxyvitamin D
assessed by using immunoassay methodology
Change in Parathyroid Hormone Level
Measured by immunoassay methodology as marker of bone metabolism
Change in High-sensitivity C-reactive Protein (Inflammatory Marker)
measured in the peripheral blood using immunoassay technique methodology
Change in Interleukin-6
Measured from fasting serum using immunoassay technique as marker of inflammation
Full Information
NCT ID
NCT02367105
First Posted
January 21, 2015
Last Updated
July 1, 2022
Sponsor
VA Office of Research and Development
Collaborators
Michael E. DeBakey VA Medical Center, Baylor College of Medicine, Biomedical Research Institute of New Mexico
1. Study Identification
Unique Protocol Identification Number
NCT02367105
Brief Title
Lifestyle Intervention and Testosterone Replacement in Obese Seniors
Acronym
LITROS
Official Title
Testosterone Replacement to Augment Lifestyle Therapy in Obese Older Veterans
Study Type
Interventional
2. Study Status
Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
February 1, 2015 (Actual)
Primary Completion Date
July 31, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
Collaborators
Michael E. DeBakey VA Medical Center, Baylor College of Medicine, Biomedical Research Institute of New Mexico
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The prevalence of obesity in Veterans is greater than in the general population, and even more so among users of the VA Health Care System. In addition, the population of obese older Veterans is rapidly increasing as more baby boomers become senior citizens. In older Veterans, obesity exacerbates the age- related decline in physical function and causes frailty which predisposes to admission to a VA chronic care facility. However, the optimal clinical approach to obesity in older adults is controversial because of the concern that weight loss therapy could be harmful by aggravating the age-related loss of muscle mass and bone mass. In fact, the MOVE (Managing Overweight/Obese Veterans) program does not have any guidelines for eligible Veterans if they are 70 or older. It is possible that the addition of testosterone replacement to lifestyle therapy will preserve muscle mass and bone mass and reverse frailty in obese older Veterans and thus prevent their loss of independence and decrease demand for VA health care services.
Detailed Description
Obesity is not only highly prevalent among Americans, but even more so among Veterans using VA medical facilities. Failure to assist Veterans in managing weight and sedentary lifestyle affects current treatment and increases future demand for VA health care services. Decreased muscle mass with aging and the need to carry extra mass due to obesity make it particularly difficult for obese older Veterans to function independently and results in frailty leading to increased nursing home admissions and increased morbidity and mortality. Data from preliminary studies showed that lifestyle therapy resulting in weight loss in this understudied population improves physical function and ameliorates frailty. However, this improvement in physical function is modest at best and most obese older adults remain physically frail. More importantly, there are concerns that lifestyle therapy may exacerbate underlying sarcopenia and osteopenia from weight loss- induced loss of lean body mass and bone mineral density (BMD). As a result, most geriatricians are reluctant to recommend lifestyle therapy that includes weight loss in obese frail elderly patients although the combination of weight loss and exercise is recommended as part of standard care for obese patients in general. Thus, it is not surprising that among Veterans, the MOVE (Managing Overweight/Obese Veterans) program does not have any guidelines for eligible Veterans if they are 70 or older. In addition to overeating and lack of exercise, age-related decline in anabolic hormone (i.e. testosterone) may contribute to sarcopenia and osteopenia, which in turn is exacerbated by obesity. Indeed, preliminary studies discovered that obese older men had markedly low levels of serum testosterone at baseline which remained low throughout the duration of lifestyle therapy. Because testosterone replacement therapy has been shown to increase muscle mass and BMD, it is therefore likely that concomitant testosterone replacement during lifestyle therapy in obese older adults would preserve lean body mass and BMD, and reverse frailty. Accordingly, the optimal management to the problem of sarcopenic obesity and frailty might require a comprehensive approach of a combination of lifestyle intervention and the correction of anabolic hormone deficiency. Therefore, the primary goal of this proposal is to conduct a randomized, comparative efficacy, double-blind, placebo-controlled (for testosterone) trial of the effects of 1) lifestyle therapy (1% diet-induced weight loss and exercise training) + testosterone replacement therapy versus 2) lifestyle therapy without testosterone replacement (testosterone placebo) in obese (BMI e 30 kg/m2) older (age e 65 yrs) male Veterans. The investigators hypothesize that 1) lifestyle therapy + testosterone replacement will cause a greater improvement in physical function than lifestyle therapy without concomitant testosterone replacement; 2) lifestyle therapy + testosterone replacement will cause a greater preservation of fat-free mass and thigh muscle volume than lifestyle therapy without testosterone replacement, 3) lifestyle therapy + testosterone replacement will cause a greater preservation in BMD and bone quality than lifestyle therapy without testosterone replacement, and 4) lifestyle therapy + testosterone replacement will cause a greater reduction in intramuscular proinflammatory cytokines than lifestyle therapy without testosterone replacement. The overarching hypothesis across aims is that a multifactorial intervention by means of lifestyle therapy plus testosterone replacement will be the most effective approach for reversing sarcopenic obesity and frailty in obese older male adults, as mediated by their additive effects in suppressing chronic inflammation, and stimulating muscle and bone anabolism. Obesity in older adults, including many aging Veterans, is a major public health problem. In fact, the public health success that has occurred in recent years could be in danger if lifestyles of older adults are neglected. The novel health outcomes and mechanistic-based data generated from this proposed randomized clinical trial (RCT) will have important ramifications for the standard of care for this rapidly increasing segment of the aging Veteran population.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity and Hypogonadism
Keywords
Obesity, Hypogonadism, Frailty
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
83 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Testosterone plus Lifestyle Therapy
Arm Type
Active Comparator
Arm Description
Testosterone replacement in combination with behavioral diet to induce ~10% weight loss + supervised aerobic and exercise training
Arm Title
Placebo plus Lifestyle Therapy
Arm Type
Placebo Comparator
Arm Description
Placebo in combination with behavioral diet to induce ~10% weight loss and supervised aerobic and exercise training
Intervention Type
Drug
Intervention Name(s)
Testosterone
Intervention Description
Daily testosterone gel applied once daily in the morning to intact skin
Intervention Type
Other
Intervention Name(s)
Lifestyle Therapy
Intervention Description
Weekly behavioral diet to induce ~10% weight loss in combination with supervised aerobic and exercise training three times a week
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo gel for testosterone
Primary Outcome Measure Information:
Title
Change in the Physical Performance Test
Description
The primary functional outcome is the modified physical performance test, which includes seven standardized tasks (walking 50 ft, putting on and removing a coat, picking up a penny, standing up from a chair, lifting a book, climbing one flight of stairs, and performing a progressive Romberg tests) plus two additional tasks (climbing up and down four flights of stairs and performing a 360-degree turn). The score for each task ranges form 0 to 4; a perfect score is 36. Higher scores indicate better physical function.
Time Frame
Baseline and 6 months
Secondary Outcome Measure Information:
Title
Change in Endurance Capacity
Description
Assessed by measuring peak oxygen consumption using indirect calorimetry during a treadmill exercise stress test
Time Frame
Baseline and 6 months
Title
Change in Functional Status
Description
Assessed by the Functional Status Questionnaire. Score range: 0 to 36 with higher scores indicating better functional status
Provides information of the participants ability to perform activities of daily living.
Time Frame
Baseline and 6 months
Title
Change in Body Weight
Description
Measured after an overnight fast using calibrated scales
Time Frame
Baseline and 6 months
Title
Change in Lean Body Mass
Description
Assessed by using dual-energy x-ray absorptiometry
Time Frame
Baseline and 6 months
Title
Change in Fat Mass
Description
Assessed by using dual-energy x-ray absorptiometry
Time Frame
Baseline and 6 months
Title
Change in Thigh Muscle Volume
Description
Assessed by using magnetic resonance imaging
Time Frame
Baseline and 6 months
Title
Thigh Fat Volume
Description
Volume of fat in the thigh by measured by magnetic resonance imaging
Time Frame
6 months
Title
Change in Total Hip Bone Mineral Density
Description
Assessed by using dual-energy x-ray absorptiometry
Time Frame
Baseline and 6 months
Title
Change in Lumbar Spine Bone Mineral Density
Description
As measured by Dual energy x-ray absorptiometry
Time Frame
Baseline and 6 months
Title
Change in Muscle Strength
Description
assessed by total1-repetition maximum (the maximal weight lifted at one time; the totals are the sum of the maximal weights lifted in the biceps curl, bench press, 387 seated row, knee extension, knee flexion, and leg press exercises).
Time Frame
Baseline and 6 months
Title
Change in Static Balance
Description
assessed by one leg limb stance
Time Frame
Baseline and 6 months
Title
Change in Dynamic Balance
Description
Assessed by using the obstacle course
Time Frame
Baseline and 6 months
Title
Change in Gait Speed
Description
Determined by measuring the time needed to walk 25 ft.
Time Frame
Baseline and 6 months
Title
Change in Composite Cognitive Z-score
Description
Test of overall cognitive performance formed by averaging the standardized scores for several domains of cognitive function (attention, memory, executive, language, global). Higher scores indicate better cognitive status.
The Z-score indicates the number of standard deviations away from the mean. A Z-score of 0 is equal to the mean of the baseline scores (units on a scale). Negative numbers indicate values lower than the reference population and positive numbers indicate values higher than the reference population
Time Frame
Baseline and 6 months
Title
Change in Modified Mini-mental Exam
Description
Test of global cognition with components for orientation, registration, attention, language, praxis, and immediate and delayed memory. Score ranges from 0 to 100 with higher scores indicate better cognition.
Time Frame
Baseline and 6 months
Title
Stroop Interference
Description
Assess the ability to inhibit cognitive interference that occurs when the processing of a specific stimulus feature impedes the simultaneous processing of a second stimulus attribute, well-known as the Stroop Effect.
Minimum score is 0, there is no maximum value. Higher scores indicate better outcome.
Time Frame
Baseline and 6 months
Title
Change in Word List Fluency
Description
Measure of verbal production, semantic memory, and language. Minimum score is 0, there is no maximum value. Higher scores indicate better outcome.
Time Frame
Baseline and 6 months
Title
Change in Ray Auditory Verbal Learning Test
Description
The Rey Auditory Verbal Learning Test (RAVLT) evaluates a wide diversity of functions: short-term auditory-verbal memory, rate of learning, learning strategies, retroactive, and proactive interference, presence of confabulation of confusion in memory processes, retention of information.
Minimum score is 0, there is no maximum value. Higher scores indicate better outcome.
Time Frame
Baseline and 6 months
Title
Change in Trail A
Description
Test of visuospatial scanning, speed of processing, mental flexibility, and executive function (with a greater focus on attention).
Minimum score is 0, there is no maximum value. Higher scores indicate better outcome.
Time Frame
Baseline and 6 months
Title
Change in Trail B
Description
Test of visuospatial scanning, speed of processing, mental flexibility, and executive function (with a focus on executive function)
Minimum score is 0, there is no maximum value. Higher scores indicate better outcome.
Time Frame
Baseline and 6 months
Title
Change in Symbol Digital Modalities Test
Description
Assesses key neurocognitive functions that underlie many substitution tasks, including attention, visual scanning, and motor speed.
Minimum score is 0, there is no maximum value. Higher scores indicate better outcome.
Time Frame
Baseline and 6 months
Title
Change in Trabecular Bone Score
Description
The trabecular bone score is a measure of bone texture correlated with bone microarchitecture and a marker for the risk of osteoporosis.
Minimum score is 0, there is no maximum value. Higher scores indicate better bone microarchitecture.
Time Frame
Baseline and 6 months
Title
Change in C-terminal Telopeptide
Description
biochemical marker of bone turnover (bone resorption) as measured by immunoassay technique
Time Frame
Baseline and 6 months
Title
Change in N-terminal Propeptide of Type I Procollagen
Description
Biochemical marker of bone turnover (bone formation) as measured by radioimmunoassay technique
Time Frame
Baseline and 6 months
Title
Change in Insulin Growth Factor-1
Description
Measured by immunoassay methodology
Time Frame
Baseline and 6 months
Title
Change in Trabecular Bone Score (Trabecular Bone Quality)
Description
assessed by trabecular bone score (TBS), a newly developed index for assessing trabecular bone quality and fracture risk.
TBS is a bone texture parameter that quantifies cancellous bone microachitecture, which is key in determining bone strength and resistance to fracture, by computing raw data from dual energy x-ray absorptiometry of the lumbar spine.
There are no minimum or maximum values. Higher scores mean better outcome.
Time Frame
Baseline and 6 months
Title
Change in Levels of 25-hydroxyvitamin D
Description
assessed by using immunoassay methodology
Time Frame
Baseline and 6 months
Title
Change in Parathyroid Hormone Level
Description
Measured by immunoassay methodology as marker of bone metabolism
Time Frame
Baseline and 6 months
Title
Change in High-sensitivity C-reactive Protein (Inflammatory Marker)
Description
measured in the peripheral blood using immunoassay technique methodology
Time Frame
Baseline and 6 months
Title
Change in Interleukin-6
Description
Measured from fasting serum using immunoassay technique as marker of inflammation
Time Frame
Baseline and 6 months
Other Pre-specified Outcome Measures:
Title
Change in Total Testosterone Levels
Description
as measured in the peripheral blood by liquid chromatography/mass spectrometry
Time Frame
Baseline and 6 months
Title
Change in Estradiol
Description
As measured by LC-MS/MS
Time Frame
Baseline and 6 months
Title
Change in Hematocrit
Description
the ratio of the volume of red blood cells to the total volume of blood.
Time Frame
Baseline and 6 months
Title
Change in Prostate Specific Antigen
Description
blood test to screen for prostate cancer
Time Frame
Baseline and 6 months
Title
Change in Short Form Health Survey (SF-36) Quality of Life Physical Component
Description
Using Short Form-36 of Life Questionnaire Physical Component subscale. Minimum score is 0, Maximum score is 100. Higher scores indicate better outcome.
Time Frame
Baseline and 6 months
Title
Change in International Prostate Symptom Score
Description
Using the International Prostate Symptom Scoring (IPS); Minimum score is 0, Maximum score is 35. Higher scores mean worse outcome.
Time Frame
Baseline and 6 months
Title
Change in Triglyceride Levels
Description
Blood samples obtained in the fasting state as part of measurements of lipid profile
Time Frame
Baseline and 6 months
Title
Change in HDL-cholesterol
Description
Blood samples obtained in the fasting state as part of measurements of lipid profile
Time Frame
Baseline and 6 months
Title
Change in Waist Circumference
Description
Waist circumference as measured horizontally at the midpoint between the highest point of the iliac crest and the lowest portion of the 12th rib in the standing position.
Time Frame
Baseline and 6 months
Title
Change in Glucose
Description
Measured in the blood after overnight fast
Time Frame
Baseline and 6 months
Title
Change in Mood
Description
Using Yesavage Depression Scale Lower scores indicate better mood (range 0 to 30).
Time Frame
Baseline and 6 months
Title
Number of Participants With Significant Changes in Functional Connectivity in the Default Mode Network
Description
Functional connectivity was measured with seeds of the DMN (medial prefrontal cortex [MPFC] and posterior cingulate cortex [PCC]). Correlation coefficients representing the degree of connectivity between hypothesized regions were Fisher transformed. An a priori threshold of p<.001 at the voxel level and p<.05, FDR corrected for multiple comparisons across the whole brain, at the cluster level were used to determine significant connectivity.
Time Frame
Baseline and 6 months
Title
Change in Skeletal Muscle Growth Factor (MYOD1)
Description
Assessed by using RNA-seq quantification of gene expression in skeletal muscles obtained during muscle biopsies.
Time Frame
Baseline and 6 months
Title
Change in Peripheral Quantitative Computed Tomography Measures (Volumetric Bone Density)
Description
assessed by quantitative computed tomography at 4% distal tibia using the following thresholds: 180 mg/cm3 and 45% of the area
Time Frame
Baseline and 6 months
10. Eligibility
Sex
Male
Gender Based
Yes
Gender Eligibility Description
Male
Minimum Age & Unit of Time
65 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subjects will be
older (65-85 yr)
obese (BMI 30 kg/m2 or greater) Veteran men with low testosterone (less than 300 mg/dL) as defined by the Endocrine Society
mild to moderately frail
must have stable weight (~not less than or more than 2 kg) during the last 6 months
sedentary (regular exercise less than 1 h/week or less than 2x/week for the last 6 months)
Exclusion Criteria:
Any major chronic diseases, or any condition that would interfere with exercise or dietary restriction, in which exercise or dietary restriction are contraindicated, or that would interfere with interpretation of results.
Examples include, but are not limited to:
cardiopulmonary disease (e.g. recent myocardial infarction (MI), unstable angina, stroke etc) or unstable disease (e.g. CHF)
severe orthopedic/musculoskeletal or neuromuscular impairments
visual or hearing impairments
cognitive impairment (Mini Mental State Exam Score less than 24)
current use of bone active drugs
uncontrolled diabetes (i.e. fasting blood glucose more than 140 mg/dl and/or HbA1c greater than 9.5%).
Any contraindications to testosterone supplementation
history of prostate or breast cancer
history of testicular disease
untreated sleep apnea
hematocrit more than 50%
prostate-related findings of palpable nodule on exam, a serum PSA of 4.0 ng/ml or greater
International Prostate Symptom Sore more than 19
history of venous thromboembolism
Osteoporosis or a BMD T-score of -2.5 in the lumbar spine or total hip as well as those patients with a history of osteoporosis-related fracture (spine, hip, or wrist)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dennis T Villareal, MD
Organizational Affiliation
Michael E. DeBakey VA Medical Center, Houston, TX
Official's Role
Principal Investigator
Facility Information:
Facility Name
Michael E. DeBakey VA Medical Center, Houston, TX
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Publications from this research will be made available to the public through the National Library of Medicine PubMed Central website within one year after the date of publication (guidance is provided on the ORD website).
MEDVAMC will not provide unrestricted, open public access to large scale health related datasets because of re-identification concerns and the obligation to protect Veterans' private information. However, controlled public access will be provided to the greatest extent possible under specific DUAs or other written agreements, and open access will be provided to the final datasets underlying peer-reviewed publications (aggregated data that can be released with privacy and confidentiality risks).
Citations:
PubMed Identifier
34375393
Citation
Gregori G, Celli A, Barnouin Y, Paudyal A, Armamento-Villareal R, Napoli N, Qualls C, Villareal DT. Cognitive response to testosterone replacement added to intensive lifestyle intervention in older men with obesity and hypogonadism: prespecified secondary analyses of a randomized clinical trial. Am J Clin Nutr. 2021 Nov 8;114(5):1590-1599. doi: 10.1093/ajcn/nqab253.
Results Reference
derived
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Lifestyle Intervention and Testosterone Replacement in Obese Seniors
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